Variant report

Variant	esv2758938
Chromosome Location	chr1:64677148-64776396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1203)
CpG islands
(count:122)
Chromatin interactive
region (count:21)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1203 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:64712027-64712366	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:64688884-64688892	K562	blood:	n/a	n/a
3	ARID3A	chr1:64708690-64708926	K562	blood:	n/a	n/a
4	ARID3A	chr1:64708548-64709072	HepG2	liver:	n/a	n/a
5	ATF1	chr1:64734761-64735082	K562	blood:	n/a	n/a
6	ATF2	chr1:64688903-64689305	GM12878	blood:	n/a	n/a
7	BACH1	chr1:64717594-64717893	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:64695384-64695391	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr1:64688957-64689391	GM12878	blood:	n/a	chr1:64689148-64689159
10	BATF	chr1:64688935-64689219	GM12878	blood:	n/a	chr1:64689148-64689159
11	BCL11A	chr1:64688947-64689318	GM12878	blood:	n/a	chr1:64689151-64689160 chr1:64689152-64689161
12	BCLAF1	chr1:64688959-64689342	GM12878	blood:	n/a	chr1:64689151-64689160 chr1:64689152-64689161
13	BHLHE40	chr1:64734841-64735094	K562	blood:	n/a	n/a
14	BHLHE40	chr1:64696852-64697039	HepG2	liver:	n/a	n/a
15	BHLHE40	chr1:64708829-64708854	K562	blood:	n/a	n/a
16	BRCA1	chr1:64734738-64735099	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr1:64688870-64689388	HCT-116	colon:	n/a	n/a
18	CBX3	chr1:64696773-64697286	HCT-116	colon:	n/a	n/a
19	CEBPB	chr1:64696835-64697303	HCT-116	colon:	n/a	n/a
20	CEBPB	chr1:64698742-64698853	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:64686765-64686906	HepG2	liver:	n/a	chr1:64686850-64686861
22	CEBPB	chr1:64686049-64686292	HepG2	liver:	n/a	chr1:64686165-64686176
23	CEBPB	chr1:64756170-64756493	K562	blood:	n/a	n/a
24	CEBPB	chr1:64720110-64720315	A549	lung:	n/a	chr1:64720176-64720187
25	CEBPB	chr1:64686080-64686226	H1-hESC	embryonic stem cell:	n/a	chr1:64686165-64686176
26	CEBPB	chr1:64700810-64701172	IMR90	lung:	n/a	chr1:64700993-64701004 chr1:64700991-64701002
27	CEBPB	chr1:64758199-64758528	IMR90	lung:	n/a	chr1:64758374-64758385 chr1:64758372-64758385 chr1:64758372-64758385 chr1:64758374-64758383 chr1:64758372-64758385 chr1:64758374-64758383 chr1:64758374-64758383 chr1:64758374-64758383
28	CEBPB	chr1:64700840-64701168	K562	blood:	n/a	chr1:64700993-64701004 chr1:64700991-64701002
29	CEBPB	chr1:64745775-64745889	A549	lung:	n/a	n/a
30	CEBPB	chr1:64700844-64701148	Hela-S3	cervix:	n/a	chr1:64700993-64701004 chr1:64700991-64701002
31	CEBPB	chr1:64774709-64774923	K562	blood:	n/a	n/a
32	CEBPB	chr1:64720006-64720336	HepG2	liver:	n/a	chr1:64720176-64720187
33	CEBPB	chr1:64677756-64678202	IMR90	lung:	n/a	n/a
34	CEBPB	chr1:64686053-64686266	K562	blood:	n/a	chr1:64686165-64686176
35	CEBPB	chr1:64700836-64701151	A549	lung:	n/a	chr1:64700993-64701004 chr1:64700991-64701002
36	CEBPB	chr1:64685997-64686329	IMR90	lung:	n/a	chr1:64686165-64686176
37	CEBPB	chr1:64688956-64689611	IMR90	lung:	n/a	n/a
38	CEBPB	chr1:64686032-64686234	Hela-S3	cervix:	n/a	chr1:64686165-64686176
39	CEBPB	chr1:64695932-64696083	A549	lung:	n/a	chr1:64695983-64695996 chr1:64695985-64695996
40	CEBPB	chr1:64696853-64697187	HCT-116	colon:	n/a	n/a
41	CEBPB	chr1:64700865-64701147	H1-hESC	embryonic stem cell:	n/a	chr1:64700993-64701004 chr1:64700991-64701002
42	CEBPB	chr1:64700817-64701164	HepG2	liver:	n/a	chr1:64700993-64701004 chr1:64700991-64701002
43	CEBPB	chr1:64698608-64698846	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr1:64695363-64695373	GM12878	blood:	n/a	n/a
45	CHD1	chr1:64689373-64689397	GM12878	blood:	n/a	n/a
46	CHD1	chr1:64734415-64735478	IMR90	lung:	n/a	n/a
47	CHD1	chr1:64713950-64714061	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr1:64734350-64734814	K562	blood:	n/a	n/a
49	CTCF	chr1:64712140-64712290	HEEpiC	esophagus:	n/a	chr1:64712195-64712216 chr1:64712200-64712218 chr1:64712201-64712217
50	CTCF	chr1:64712120-64712270	HFF-Myc	foreskin:	n/a	chr1:64712195-64712216 chr1:64712200-64712218 chr1:64712201-64712217

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:64711033-64711083	HUVEC	blood vessel:	n/a
2	chr1:64689428-64689478	ECC-1	luminal epithelium:	n/a
3	chr1:64689428-64689478	BJ	skin:	n/a
4	chr1:64689428-64689478	MCF10A-Er-Src	breast:	n/a
5	chr1:64711033-64711083	NB4	blood:	n/a
6	chr1:64689428-64689478	U87	brain:	n/a
7	chr1:64689428-64689478	HEEpiC	esophagus:	n/a
8	chr1:64689428-64689478	PANC-1	pancreas:	n/a
9	chr1:64711033-64711083	NHBE	bronchial:	n/a
10	chr1:64689428-64689478	HRCEpiC	kidney:	n/a
11	chr1:64689428-64689478	PFSK-1	brain:	n/a
12	chr1:64711033-64711083	SK-N-MC	brain:	n/a
13	chr1:64711033-64711083	GM12878	blood:	n/a
14	chr1:64689428-64689478	Caco-2	colon:	n/a
15	chr1:64689428-64689478	BE2_C	brain:	n/a
16	chr1:64711033-64711083	MCF-7	breast:	n/a
17	chr1:64689428-64689478	Hela-S3	cervix:	n/a
18	chr1:64689428-64689478	HNPCEpiC	eye:	n/a
19	chr1:64689428-64689478	HRPEpiC	eye:	n/a
20	chr1:64711033-64711083	U87	brain:	n/a
21	chr1:64711033-64711083	Caco-2	colon:	n/a
22	chr1:64689428-64689478	SKMC	muscle:	n/a
23	chr1:64711033-64711083	HCT-116	colon:	n/a
24	chr1:64689428-64689478	NHBE	bronchial:	n/a
25	chr1:64689428-64689478	HCPEpiC	choroid plexus:	n/a
26	chr1:64711033-64711083	SK-N-SH	brain:	n/a
27	chr1:64711033-64711083	HEEpiC	esophagus:	n/a
28	chr1:64711033-64711083	LNCaP	prostate:	n/a
29	chr1:64689428-64689478	SK-N-SH	brain:	n/a
30	chr1:64689428-64689478	SAEC	small airway:	n/a
31	chr1:64711033-64711083	AG09309	skin:	n/a
32	chr1:64711033-64711083	GM12891	blood:	n/a
33	chr1:64689428-64689478	AG04449	skin:	fetal
34	chr1:64689428-64689478	T-47D	breast:	n/a
35	chr1:64711033-64711083	HIPEpiC	eye:	n/a
36	chr1:64689428-64689478	CMK	blood:	n/a
37	chr1:64689428-64689478	AoSMC	blood vessel:	n/a
38	chr1:64711033-64711083	AG04450	lung:	fetal
39	chr1:64711033-64711083	HAEpiC	amniotic membrane:	n/a
40	chr1:64689428-64689478	SK-N-MC	brain:	n/a
41	chr1:64689428-64689478	AG10803	skin:	n/a
42	chr1:64711033-64711083	Hepatocyte	liver:	n/a
43	chr1:64711033-64711083	T-47D	breast:	n/a
44	chr1:64711033-64711083	BE2_C	brain:	n/a
45	chr1:64689428-64689478	NHDF-neo	bronchial:	n/a
46	chr1:64689428-64689478	AG04450	lung:	fetal
47	chr1:64711033-64711083	SK-N-SH_RA	brain:	n/a
48	chr1:64711033-64711083	ProgFib	skin:	n/a
49	chr1:64711033-64711083	SAEC	small airway:	n/a
50	chr1:64711033-64711083	HRCEpiC	kidney:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:64734478..64735394-chr1:64952477..64953272,5	MCF-7	breast:
2	chr1:64022770..64023546-chr1:64711686..64712434,2	MCF-7	breast:
3	chr1:64682305..64684048-chr1:64684214..64686001,2	K562	blood:
4	chr1:64734478..64735120-chr1:65289561..65290560,5	K562	blood:
5	chr1:64081135..64082186-chr1:64711744..64712683,6	K562	blood:
6	chr1:64734513..64735365-chr1:64952428..64953070,5	MCF-7	breast:
7	chr1:64753452..64756020-chr1:64760249..64761940,2	K562	blood:
8	chr1:64081555..64082189-chr1:64710482..64711134,2	K562	blood:
9	chr1:64744489..64747254-chr1:64749124..64750884,2	K562	blood:
10	chr1:64747599..64749584-chr1:64752328..64754322,2	MCF-7	breast:
11	chr1:64139816..64140721-chr1:64711774..64712695,4	K562	blood:
12	chr1:64747599..64749584-chr1:64752328..64754322,2	MCF-7	breast:
13	chr1:64734683..64735627-chr1:65141295..65142053,3	MCF-7	breast:
14	chr1:64081527..64082232-chr1:64708388..64709177,2	MCF-7	breast:
15	chr1:64081408..64082153-chr1:64708620..64709264,2	MCF-7	breast:
16	chr1:64081131..64082205-chr1:64708460..64709354,4	K562	blood:
17	chr1:64744489..64747254-chr1:64749124..64750884,2	K562	blood:
18	chr1:64753452..64756020-chr1:64760249..64761940,2	K562	blood:
19	chr1:64734473..64734993-chr1:64829195..64829695,2	MCF-7	breast:
20	chr1:64682305..64684048-chr1:64684214..64686001,2	K562	blood:
21	chr1:64139834..64140680-chr1:64710715..64711737,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ROR1-3	chr1:64707335-64707416	NONHSAT003707
2	lnc-ROR1-3	chr1:64686542-64686590	NONHSAT003707
3	lnc-ROR1-3	chr1:64698244-64698332	NONHSAT003707
4	lnc-ROR1-3	chr1:64681136-64681208	NONHSAT003707
5	lnc-ROR1-3	chr1:64709813-64710023	NONHSAT003707

No data

Variant related genes	Relation type
UBE2U	TF binding region
UBE2U	CpG island

Extended variants
information (count: 2914 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2914 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566238953	chr1:64677166-64677167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527421604	chr1:64677185-64677186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559833337	chr1:64677189-64677190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567176679	chr1:64677203-64677204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12096887	chr1:64677271-64677272	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs137917375	chr1:64677296-64677297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571492842	chr1:64677307-64677308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538842019	chr1:64677340-64677341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34931363	chr1:64677367-64677368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12097017	chr1:64677555-64677556	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs548708993	chr1:64677588-64677589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111709619	chr1:64677599-64677600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369186958	chr1:64677604-64677605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs825177	chr1:64677606-64677607	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs112345021	chr1:64677642-64677643	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs112812964	chr1:64677645-64677646	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs67777472	chr1:64677649-64677650	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs554819501	chr1:64677654-64677655	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs369490989	chr1:64677673-64677674	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs552356319	chr1:64677684-64677685	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs147541608	chr1:64677763-64677764	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs568360991	chr1:64677795-64677796	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs7546938	chr1:64677853-64677854	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs78295428	chr1:64677877-64677878	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs140153150	chr1:64677887-64677888	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs560359333	chr1:64677910-64677911	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs78789638	chr1:64677948-64677949	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs570038419	chr1:64677953-64677954	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs548837172	chr1:64677995-64677996	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs561006324	chr1:64678078-64678079	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs114501912	chr1:64678114-64678115	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs76390514	chr1:64678121-64678122	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs571462745	chr1:64678174-64678175	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs35554046	chr1:64678186-64678187	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs547711244	chr1:64678233-64678234	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs75133470	chr1:64678265-64678266	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs536436151	chr1:64678288-64678289	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs535103176	chr1:64678300-64678301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs117406482	chr1:64678374-64678375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574031181	chr1:64678424-64678425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571067715	chr1:64678425-64678426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372591603	chr1:64678464-64678465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537861072	chr1:64678519-64678520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375098905	chr1:64678550-64678551	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs577609590	chr1:64678594-64678595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375370814	chr1:64678604-64678605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534905084	chr1:64678625-64678626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553488459	chr1:64678629-64678630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75619971	chr1:64678652-64678653	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs12723442	chr1:64678701-64678702	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:64676000-64679200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr1:64676000-64679200	Enhancers	Muscle Satellite Cultured Cells	--
3	chr1:64676200-64679000	Enhancers	NHDF-Ad	bronchial
4	chr1:64676400-64679200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:64676800-64677200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr1:64676800-64678600	Enhancers	NHLF	lung
7	chr1:64676800-64679200	Enhancers	Osteobl	bone
8	chr1:64677000-64677200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:64677000-64677200	Enhancers	HSMM	muscle
10	chr1:64677000-64677400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:64677000-64677600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:64677000-64678200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr1:64677200-64677800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:64677200-64678000	Weak transcription	HSMM	muscle
15	chr1:64677200-64678600	Enhancers	NH-A	brain
16	chr1:64677400-64678200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:64677800-64678200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:64677800-64678200	Enhancers	NHEK	skin
19	chr1:64677800-64678400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr1:64678000-64678200	Enhancers	Aorta	Aorta
21	chr1:64678000-64678200	Enhancers	HSMMtube	muscle
22	chr1:64678000-64679000	Enhancers	HSMM	muscle
23	chr1:64678400-64688800	Weak transcription	HSMMtube	muscle
24	chr1:64679200-64685800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr1:64679200-64686000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:64679200-64688200	Weak transcription	Osteobl	bone
27	chr1:64679800-64682600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:64681200-64681800	Enhancers	Fetal Kidney	kidney
29	chr1:64681400-64681800	Enhancers	Placenta	Placenta
30	chr1:64681800-64686800	Weak transcription	Placenta	Placenta
31	chr1:64682600-64683200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:64683200-64686000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:64685800-64686400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:64685800-64686400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr1:64686000-64686200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:64686000-64686200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:64686000-64686400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:64686200-64687400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:64686200-64689400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:64686400-64688000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:64686400-64688200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:64686400-64688400	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr1:64686400-64688600	Weak transcription	NHDF-Ad	bronchial
44	chr1:64686800-64687400	Enhancers	Placenta	Placenta
45	chr1:64687400-64687800	Weak transcription	Placenta	Placenta
46	chr1:64687800-64688600	Enhancers	Placenta	Placenta
47	chr1:64688000-64690800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:64688200-64689400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:64688200-64690600	Enhancers	Osteobl	bone
50	chr1:64688400-64690200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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